37 Results for "

sedative agent

" in MedChemExpress (MCE) Product Catalog:
Products (37)

37 Results for "sedative agent" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-N1919
CAS No.: 483-04-5
Synonyms: Raubasine
Ajmalicine (Raubasine) is a potent adrenolytic agent which preferentially blocks α1-adrenoceptor. Ajmalicine is an reversible but non-competitive nicotine receptor full inhibitor, with an IC50 of 72.3 μM. Ajmalicine also can be used as anti-hypertensive, and serpentine, with sedative activity .
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1
1 Cited Publications
Cat. No.: HY-N2059
CAS No.: 11031-45-1
Santalol is a mixture of α and β-isomer santalol. α-Santalol is found in sandalwood oil. α-Santalol is a promising anti-cancer agent against cancers such as oral, breast, prostate and skin cancer. Santalol has sedative activity .
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Cat. No.: HY-14785
CAS No.: 208110-64-9
Purity:  99.20%
Synonyms: NLX-112; F13640
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Befiradol (NLX-112) is a highly selective 5-HT1A receptor agonist that acts on both presynaptic and postsynaptic sites. Befiradol attenuates sedative agent-induced respiratory depression in neonatal and adult rats. Befiradol reduces the duration of sedative agent-induced analgesia and sedation in adult rats. Befiradol can be used in studies related to opioid-induced respiratory depression .
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Cat. No.: HY-18715
CAS No.: 166734-83-4
Synonyms: (S)-Ornidazole; Levornidazole
Levo-ornidazole ((S)-Ornidazole) is the L-isomer of Ornidazole. Ornidazole (Levo-) increases GAD 65/67 expression and decreases brain Glu/GABA ratio. Ornidazole (Levo-) has a mild sedative effect. Levo-ornidazole can be used in the research of anti-anaerobic and anti-parasitic agents .
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Cat. No.: HY-B0971
CAS No.: 132-20-7
Synonyms: Prophenpyridamine maleate; Tripoton maleate
Pheniramine (Prophenpyridamine; Tripoton) maleate is a first-generation histamine H1 receptor antagonist, acts on the central nervous system (CNS) with sedative and hypnotic effect. Pheniramine maleate displays antitumor effect and induces leukemia cells apoptosis. Pheniramine maleate is also a safe and effective local agent that can suppress or relieve pain, with antipruritic effects .
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Cat. No.: HY-12394
CAS No.: 113-53-1
Purity:  98.22%
Synonyms: Dosulepin; Dothep
Research Areas:  

Neurological Disease

Dothiepin (Dosulepin; Dothep) is an antidepressant agent with sedative/anxiolytic activity. Dothiepin is an inhibitor preferring of noradrenaline uptake than serotonin uptake. Dothiepin facilitates noradrenergic neurotransmission via inhibiting the neuronal uptake. Dothiepin is also an antagonist of histamine H1-receptor without cardiotoxicity. Dothiepin exhibits significant analgesic activity in psychogenic facial pain,idiopathic fibromyalgia syndrome or rheumatoid arthritis .
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Cat. No.: HY-135735A
CAS No.: 190000-46-5
Synonyms: (R)-Dexmedetomidine hydrochloride; (-)-Medetomidine hydrochloride; (R)-Medetomidine hydrochloride
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

Levomedetomidine hydrochloride is an isomer of Medetomidine (HY-17034), and a cardioprotective agent with sedative and analgesic effects .
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Cat. No.: HY-B1316
CAS No.: 635-41-6
Target:  

Fungal

Research Areas:  

Infection Neurological Disease

Trimetozine is an Antifungal agent and sedative. Trimetozine exhibits antibacterial activity against Candida albicans, Candida glabrata, and Miconazole (HY-B0454)-resistant Candida glabrata cultures. Trimetozine exerts a sedative effect. Trimetozine can be used in research related to candidiasis and anxiety disorders .
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Cat. No.: HY-B1733
CAS No.: 92-12-6
Synonyms: Bistrimin; Histionex
Phenyltoloxamine (Bistrimin) is an antihistamine agent with sedative and analgesic effects. Phenyltoloxamine also has potent Sigma-1 receptor binding affinity (Ki: 160 nM) .
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Cat. No.: HY-174422
CAS No.: 676494-79-4
Target:  

Opioid Receptor

Research Areas:  

Others

Opioid receptor antagonist 2 (Compound 9) is a potent opioid receptor antagonist. Opioid receptor antagonist 2 can reverse ventilatory depression and vocal cord closure induced by sedative agent analogs in mice. Opioid receptor antagonist 2 is promising for research of acute poisoning such as respiratory depression caused by overdose of opioids .
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Cat. No.: HY-B0971A
CAS No.: 86-21-5
Synonyms: Prophenpyridamine; Tripoton; Pheniramine solution
Pheniramine (Prophenpyridamine;Tripoton) is a first-generation histamine H1 receptor antagonist, acts on the central nervous system (CNS) with sedative and hypnotic effect. Pheniramine displays antitumor effect and induces leukemia cells apoptosis. Pheniramine is also a safe and effective local agent that can suppress or relieve pain, with antipruritic effects .
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Cat. No.: HY-100377
CAS No.: 82351-05-1
Purity:  99.48%
Synonyms: Anticonvulsant 7903
Target:  

Others

Research Areas:  

Neurological Disease

Lvguidingan is a potent anticonvulsant agent. Lvguidingan also has sedative-hypnotic, tranquilizing, and muscle-relaxing actions. Lvguidingan can be used as antiepileptic agent .
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Cat. No.: HY-14785A
CAS No.: 2436760-81-3
Purity:  99.93%
Synonyms: NLX-112 hydrochloride; F 13640 hydrochloride
Target:  

5-HT Receptor

Befiradol (NLX-112) hydrochloride is a highly selective 5-HT1A receptor agonist that acts on both presynaptic and postsynaptic sites. Befiradol hydrochloride attenuates sedative agent-induced respiratory depression in neonatal and adult rats. Befiradol reduces the duration of sedative agent-induced analgesia and sedation in adult rats. Befiradol hydrochloride can be used in studies related to opioid-induced respiratory depression .
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Cat. No.: HY-N1919R
CAS No.: 483-04-5
Synonyms: Raubasine (Standard)
Ajmalicine (Standard) is the analytical standard of Ajmalicine. This product is intended for research and analytical applications. Ajmalicine (Raubasine) is a potent adrenolytic agent which preferentially blocks α1-adrenoceptor. Ajmalicine is an reversible but non-competitive nicotine receptor full inhibitor, with an IC50 of 72.3 μM. Ajmalicine also can be used as anti-hypertensive, and serpentine, with sedative activity .
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Cat. No.: HY-155297
CAS No.: 55248-23-2
Synonyms: FLA-136
Target:  

Histamine Receptor

Research Areas:  

Cardiovascular Disease

Nebidrazine is a centrally-acting hypotensive agent compared to clonidine, demonstrating weaker cardiovascular effects in rats. It induces dose-dependent hypotension and bradycardia when administered intracerebroventricularly (i.c.v.), with significantly lower sedative potential than clonidine in conscious rats. Yohimbine attenuates the cardiovascular effects of both Nebidrazine and clonidine, suggesting involvement of central alpha-autoreceptors sensitive to yohimbine. Unlike clonidine, Nebidrazine does not affect peripheral alpha-adrenoceptors in pithed rats, indicating a selective central mechanism. Chemical sympathectomy reduces Nebidrazine's cardiovascular effects more than clonidine's, and metiamide diminishes responses to both drugs, implicating central histamine receptors. These findings highlight Nebidrazine's distinct pharmacological profile and potential therapeutic application in managing hypertension through central alpha-autoreceptor stimulation .
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Cat. No.: HY-120474
CAS No.: 98601-60-6
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

Ro 23-0364 is an oral active imidazobenzodiazepine agent with mixed benzodiazepine. Ro 23-0364 shows sedative and can be used for study of neurological disease .
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Cat. No.: HY-B1375
CAS No.: 77-04-3
Target:  

c-Fms

Research Areas:  

Neurological Disease

Pyrithyldione is a sedative-hypnotic agent that induces agranulocytosis .
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Cat. No.: HY-119461
CAS No.: 5579-13-5
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

Capuride is an orally active sedative agent. Capuride has anticonvulsant activity .
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Cat. No.: HY-121918
CAS No.: 134377-22-3
Target:  

Others

Research Areas:  

Others

RU 41656 partially alleviated triazolam-induced memory impairment but did not counteract the sedative effects of this agent .
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Cat. No.: HY-B1504
CAS No.: 77-66-7
Synonyms: Acetylcarbromal
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

Acecarbromal (Acetylcarbromal) is a Urea (HY-Y0271) derivative. Acecarbromal is a hypnotic and sedative agent .
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